DNA

Part:BBa_K5443003:Experience

Designed by: Nick Coleman, Carmen Hawthorne   Group: iGEM24_MacquarieUni   (2024-09-27)
Revision as of 11:26, 2 October 2024 by Nickcoleman (Talk | contribs)

We succeeded in producing a relatively large amount of caffeate (35 ppm) relative to the other metabolites, and thus we can conclude that the enzyme Parts in the plasmid pMQ3C-11 were all at least partially functional, including the 4-Coumarate 3-Hydroxylase C3H-HpaBC. See LC-MS data below (Fig. 1).


Figure 1. LCMS analysis of compounds produced using pMQ3C-11.
The graph shows the detected presence of all 6 tested compounds, validating successful expression of all parts within pMQ3C-11.



Figure 2. Patched clones of plasmid variants.
Each plate shows patched colonies transformed with variants of our created plasmids pMQ3B and pMQ3C. Some patched colonies show diffusion of a brown pigment into the surrounding agar, suggesting a side-reaction of the enzyme HpaBC that produces the brown pigment L-DOPA.


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